Search for dissertations about: "processive"
Showing result 1 - 5 of 15 swedish dissertations containing the word processive.
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1. Towards a semantics of linguistic time : exploring some basic time concepts with special reference to English and Krio
Abstract : Using English and the West-African creole language Krio as the objects of investigation, this study proposes an analysis in which verbs and the paradigms pertaining to verbs are conceived of as being the only direct carriers of linguistic time encoding. The fundamental assumption is that nominals encode substance, be it concrete or abstract, and that verbals encode abstract substance with time. READ MORE
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2. Poly(A)-Specific Ribonuclease (PARN)
Abstract : Degradation of the mRNA 3'-end located poly(A) tail is an important step for mRNA decay in mammalian cells. Thus, to understand mRNA decay in detail, it is important to identify the catalytic activities involved in degrading poly(A). READ MORE
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3. PARN – The Tail End : Function and mechanisms of specificity and processivity
Abstract : Poly(A)-specific ribonuclease (PARN) is an exoribonuclease that is processive, poly(A) specific and cap-binding. PARN deadenylates the poly(A) tails present on a subset of mRNAs and non-coding RNAs, including among others certain snoRNAs, miRNAs and precursor rRNAs. READ MORE
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4. Cellulose hydrolysis by Trichoderma reesei cellulases: Studies on adsorption, sugar production and synergism of cellobiohydrolase I, II and endoglucanase II
Abstract : Three major cellulases, cellobiohydrolase I and II (CBH I and II) and endoglucanase II (EG II) of Trichoderma reesei have been purified by ion-exchange chromatography in an FPLC system. Microcrystalline cellulose (Avicel) was hydrolysed by the single enzymes and by equimolar mixtures of CBH I-CBH II and CBH I-EG II. READ MORE
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5. Kinetic assays for RNA-cleaving deoxyribozymes and other nucleases
Abstract : In this thesis two different assays for real-time RNA-cleaving deoxyribozyme and general nuclease kinetics are presented. Previous publications on nuclease kinetic assays have been riddled with drawbacks of labeling, discontinuity, cost etc. READ MORE